A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033718



Internal ID19122939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179401776..179427294hg38UCSC Ensembl
Innerchr4:180322930..180348448hg19UCSC Ensembl
Innerchr4:180559924..180585442hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3825519
hg1925519
hg1825519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744527, nssv3635564
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033718
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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